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Djo Surgical

FDA UDI

Class III (US FDA UDI)

by Encore Medical, L.p.

Identity

Trade Name
DJO SURGICAL FDA UDI
Generic Name
Press-fit femoral stem prosthesis FDA UDI
Device Name
HIP, STEM, CLP, REVISION, SIZE#12, IMPLANT, POLISHED NECK FDA UDI
Model / Reference
426-12-120 FDA UDI
Description
HIP, STEM, CLP, REVISION, SIZE#12, IMPLANT, POLISHED NECK FDA UDI

Identifiers

Primary DI / UDI-DI
00888912079846 FDA UDI
510(k) Number
K052320 FDA UDI
FDA Product Code
KWA FDA UDI
KWL FDA UDI
LWJ FDA UDI
KWY FDA UDI
LPH FDA UDI
LZO FDA UDI
JDI FDA UDI
KWZ FDA UDI
GMDN Term
Press-fit femoral stem prosthesis FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
888.3330 FDA UDI
888.3360 FDA UDI
888.3390 FDA UDI
888.3358 FDA UDI
888.3353 FDA UDI
888.3350 FDA UDI
888.3310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Press-fit femoral stem prosthesis

Djo Surgical by Encore Medical, L.p. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit femoral stem prosthesis.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 383840a7-f9f4-42b9-ba1c-07308ac54001 34 fields · synced May 31, 2026